Canonical Allele Identifier: CA1929388175

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067223_95067226delinsACTC , CM000672.2:g.95067223_95067226delinsACTC	GRCh38
NC_000010.10:g.96826980_96826983delinsACTC , CM000672.1:g.96826980_96826983delinsACTC	GRCh37
NC_000010.9:g.96816970_96816973delinsACTC	NCBI36
NG_007972.1:g.7272_7275delinsGAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.463_466delinsGAGT MANE Select	ENSP00000360317.3:p.Glu155=
ENST00000371270.5:c.463_466delinsGAGT	ENSP00000360317.3:p.Glu155=
ENST00000479946.2:n.767_770delinsGAGT
ENST00000490994.6:c.*249_*252delinsGAGT	ENSP00000433314.1:n.*249_*252delinsGAGT
ENST00000525991.5:c.*38_*41delinsGAGT	ENSP00000433842.1:n.*38_*41delinsGAGT
ENST00000526814.5:n.718_721delinsGAGT
ENST00000527420.5:c.463_466delinsGAGT	ENSP00000433191.1:p.Glu155=
ENST00000527953.5:n.718_721delinsGAGT
ENST00000533320.5:n.697_700delinsGAGT
ENST00000535898.5:c.157_160delinsGAGT	ENSP00000445062.1:p.Glu53=
ENST00000539050.5:c.253_256delinsGAGT	ENSP00000442343.2:p.Glu85=
ENST00000623108.3:c.253_256delinsGAGT	ENSP00000485110.1:p.Glu85=
ENST00000628935.1:c.205_208delinsGAGT	ENSP00000487145.1:p.Glu69=
NM_000770.3:c.463_466delinsGAGT MANE Select	NP_000761.3:p.Glu155=
NM_001198853.1:c.253_256delinsGAGT	NP_001185782.1:p.Glu85=
NM_001198854.1:c.157_160delinsGAGT	NP_001185783.1:p.Glu53=
NM_001198855.1:c.253_256delinsGAGT	NP_001185784.1:p.Glu85=
XR_945610.1:n.559_562delinsGAGT